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Catalog Number:
33594
CAS Number:
1212966-63-6
2-Chloro-4-fluoro-D-phenylalanine
Synonym(s):
D-Phe(2-Cl,4-F)-OH, (R-2-Amino-2-chloro-4-fluorophenylpropionic acid, H-D-Phe(2-Cl,4-F)-OH
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$58.39 /100MG
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Product Information

2-Chloro-4-fluoro-D-phenylalanine is a specialized amino acid derivative that has garnered attention in pharmaceutical research and development. This compound is recognized for its unique structural features, which include a chlorine and fluorine substituent on the phenyl ring, enhancing its reactivity and potential as a building block in drug synthesis. Researchers have utilized 2-Chloro-4-fluoro-D-phenylalanine in the design of novel therapeutic agents, particularly in the fields of neuropharmacology and cancer treatment, where its ability to mimic natural amino acids can be leveraged to influence biological pathways.

The compound's distinct properties make it an excellent candidate for incorporation into peptide synthesis and medicinal chemistry applications. Its fluorinated structure can improve the metabolic stability of peptides, making them more effective in therapeutic contexts. Additionally, 2-Chloro-4-fluoro-D-phenylalanine serves as a valuable tool for studying protein interactions and enzyme mechanisms, providing insights that can lead to the development of innovative treatments. This compound stands out in the realm of amino acid derivatives, offering researchers a versatile option for advancing their projects.

Synonyms
D-Phe(2-Cl,4-F)-OH, (R-2-Amino-2-chloro-4-fluorophenylpropionic acid, H-D-Phe(2-Cl,4-F)-OH
CAS Number
1212966-63-6
Molecular Formula
C9H9ClFNO2
Molecular Weight
217.63
MDL Number
MFCD12198161
PubChem ID
15926053
Conditions
Store at 2 - 8 °C
General Information
Synonyms
D-Phe(2-Cl,4-F)-OH, (R-2-Amino-2-chloro-4-fluorophenylpropionic acid, H-D-Phe(2-Cl,4-F)-OH
CAS Number
1212966-63-6
Molecular Formula
C9H9ClFNO2
Molecular Weight
217.63
MDL Number
MFCD12198161
PubChem ID
15926053
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-4-fluoro-D-phenylalanine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a building block in the synthesis of novel drugs, particularly in the development of treatments for neurological disorders.
  • Biochemical Research: It is used in studies investigating protein interactions and enzyme activity, helping researchers understand metabolic pathways and disease mechanisms.
  • Peptide Synthesis: The compound is valuable in creating modified peptides, which can enhance the efficacy and specificity of therapeutic agents.
  • Drug Design: Its unique structure allows for the exploration of structure-activity relationships, aiding in the design of more effective pharmaceuticals with fewer side effects.
  • Academic Research: It is commonly employed in academic laboratories for teaching purposes, demonstrating concepts in organic chemistry and medicinal chemistry.

Citations